反応式
[CH2:1]([O:3][C:4]1[CH:14]=[CH:13][CH:12]=[CH:11][C:5]=1[C:6](OCC)=[O:7])[CH3:2].O.[NH2:16][NH2:17]>C(O)C>[CH2:1]([O:3][C:4]1[CH:14]=[CH:13][CH:12]=[CH:11][C:5]=1[C:6]([NH:16][NH2:17])=[O:7])[CH3:2]参加物
4
実験手順
Ethyl 2-ethoxybenzoate (100 g, 128.7 mmol) and hydrazine hydrate (100%, 25 ml, 128.7 mmol) are dissolved in 200 ml of ethanol and heated under reflux for 5 hours. A further 12.5 ml (64.3 mmol) of hydrazine hydrate are added and the reaction mixture is heated under reflux for a further 7 hours. For working up, the reaction mixture is extensively concentrated and then stirred with 300 ml of cyclohexane at room temperature. After cooling to 0° C., the crystals are filtered off with suction, washed twice with 50 ml of cold cyclohexane each time and finally dried in a vacuum oven at 35° C. and 300 mbar overnight.
後処理
- temperatureheated
- temperatureunder reflux for 5 hours
- temperaturethe reaction mixture is heated
- temperatureunder reflux for a further 7 hours
- concentrationthe reaction mixture is extensively concentrated
- temperatureAfter cooling to 0° C.
- filtrationthe crystals are filtered off with suction
- washwashed twice with 50 ml of cold cyclohexane each time
- customfinally dried in a vacuum oven at 35° C.
- custom300 mbar overnight
出典と根拠
- ORDレコード
- ord-6c73366988844741950c23fb20734acd
- 出典データセット
- uspto-grants-2006_04
- 特許番号
- US07022847B2
関連ノート
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